Gallamine Triethiodide Gallamine Triethiodide

Structural formula

• Numbering system
• Physical property data
• Toxicological data
• Ecological data
• Molecular structure data
• Computing chemical data
• More
  • Properties and Stability
  • Storage method
  • Synthesis method
  • Purpose

Numbering system

CAS number:65-29-2

MDL number:MFCD00011832

EINECS number:200-605-1

RTECS number:BS1100000

BRN number:None

PubChem number:24277837

Physical property data

1. Character:White or milky white crystalline powder, odorless, slightly bitter, hygroscopic

2. Density (g/mL,25/4℃): Unsure

3. Relative vapor density (g/mL,AIR=1): Unsure

4. Melting point (ºC):235 (dec.)(lit.)

5. Boiling point (ºC,Normal pressure): Uncertain

6. Boiling point (ºC, 5.2kPa): Unsure

7. Refractive index:Not sure

8. Flash point (ºC): Unsure

9. Specific optical rotation (º): Unsure

10. Autoignition point or ignition temperature (ºC): Unsure

11. Vapor pressure (kPa,25ºC): Unsure

12. 17. Explosion limit (%, V/V): Unsure

18. Lower explosion limit (%,V/V): Unsure

19. Solubility:Easily soluble in water(1：6), slightly soluble in Ethanol(1：500), acetone, benzene and chloroform, insoluble in ether

Toxicological data

None yet

Ecological data

None yet

Molecular structure data

None yet

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 6

4. Number of rotatable chemical bonds: 21

5. Number of tautomers: none

6. Topological molecule polar surface area 27.7

7. Number of heavy atoms: 39

8. Surface charge: 0

9. Complexity: 489

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 4

Properties and stability

None yet

Storage method

This product should be sealed in4℃Save in a dry place and away from light.

Synthesis method

Pyrogallic acid forms a sodium salt under the action of sodium acetate , and then reacted with diethylaminoethyl chloride and ethyl iodide in sequence.

Purpose

For biochemical research. medicine.

eft> This product should be sealed in 4℃Keep dry and away from light.

Synthesis method

Pyrogallic acid forms a sodium salt under the action of sodium acetate , and then reacted with diethylaminoethyl chloride and ethyl iodide in sequence.

Purpose

For biochemical research. medicine.